FDA 510(k)

I.V. Administration Set, I.V. Extension Set

N.º K: K223645 · 2023-05-18

Fecha de decisión2023-05-18

Código de productoFPA

Comité asesorHO

DecisiónSubstantially Equivalent

Resumen del dispositivo

I.V. Administration Set, I.V. Extension Set is the device name listed in this FDA 510(k) record. The listed applicant is Bq Plus Medical Co., Ltd.. It received FDA 510(k) clearance on 2023-05-18 under 510(k) number K223645. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the I.V. Administration Set, I.V. Extension Set?

I.V. Administration Set, I.V. Extension Set is a medical device that received FDA 510(k) clearance on 2023-05-18. The listed applicant is Bq Plus Medical Co., Ltd.. The 510(k) number is K223645.

When did I.V. Administration Set, I.V. Extension Set receive FDA 510(k) clearance?

I.V. Administration Set, I.V. Extension Set received FDA 510(k) clearance on 2023-05-18, under 510(k) number K223645.

Who is the listed applicant for I.V. Administration Set, I.V. Extension Set?

The FDA 510(k) record lists Bq Plus Medical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for I.V. Administration Set, I.V. Extension Set?

The FDA product code for I.V. Administration Set, I.V. Extension Set is FPA.

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Otros registros que enlistan a Bq Plus Medical Co., Ltd. como solicitante

K242126I.V. Administration Set K210381I.V. Administration Set

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Fuente oficial

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Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.